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首页> 外文期刊>Brain & Development >An 8-year-old boy with vertebral artery dissection with cerebellar ataxia featuring suspected vertebral artery hypoplasia.
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An 8-year-old boy with vertebral artery dissection with cerebellar ataxia featuring suspected vertebral artery hypoplasia.

机译:一个8岁男孩,椎动脉夹层合并小脑性共济失调,可疑为椎动脉发育不全。

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We report an 8-year-old boy with left vertebral artery dissection featuring cerebellar ataxia in which congenital vertebral artery hypoplasia was suspected as a predisposing factor in the dissection. The patient suddenly suffered from vertigo and vomiting while swimming, and he was brought to our department. The initial brain Computed Tomography (CT) demonstrated no abnormalities, and his symptoms disappeared the next morning. However, one month after onset, brain Magnetic Resonance Imaging (MRI) revealed ischemic changes (infarction) in the left cerebellum. Transfemoral angiography showed complete occlusion at the C2 portion of the left vertebral artery, suggesting dissection and diffuse narrowing of the proximal segment of the occlusion site. Three-dimensional CT angiography also revealed diffuse narrowing of the left vertebral artery from the bifurcation of the subclavian artery. He has since been living daily life without any difficulties. The detailed etiology of cerebral artery dissection remainsunknown, but arterial anomalies should be considered as a predisposing factor.
机译:我们报告了一个8岁男孩,患有小脑性共济失调的左椎动脉夹层,其中先天性椎动脉发育不全被怀疑是该夹层的诱因。该患者在游泳时突然出现眩晕和呕吐,被带到我们部门。最初的脑部计算机断层扫描(CT)没有显示异常,第二天早上他的症状消失了。然而,发病后一个月,脑磁共振成像(MRI)显示左小脑缺血性改变(梗塞)。经股血管造影显示左椎动脉C2部分完全闭塞,提示闭塞位点近端段解剖并弥漫变窄。三维CT血管造影还显示,锁骨下动脉分叉导致左椎动脉弥漫性变窄。此后,他一直没有任何困难地过着日常生活。脑动脉夹层的详细病因仍未知,但应将动脉异常视为诱发因素。

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